利用微悬臂梁传感对瘦肉精进行非标记检测
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国家重点基础研究发展计划(2006CB300404);国家自然科学基金(10627201和10732080)


Label-free detection of clenbuterol based on microcantilever
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    摘要:

    目的 利用微悬臂梁传感技术对瘦肉精抗原抗体的特异性结合进行检测。 方法 将巯基化的瘦肉精抗体通过自组装修饰到微悬臂梁的金面,在加入不同浓度的瘦肉精标准样品的过程中,通过光杠杆原理监测微悬臂梁的实时弯曲信号。巯基化瘦肉精抗体的活性和微悬臂梁上抗原抗体的结合得到酶联免疫吸附(ELISA)实验的验证。结果 该系统能够检测至少1ng/ml浓度的瘦肉精标准样品,而且具有很强的选择性,在对照实验中加入不含瘦肉精的1μg/ml氯霉素溶液没有响应。另外,瘦肉精抗原抗体的结合导致微悬臂梁产生压应力,而且微悬臂梁表面应力的改变与样品浓度的对数成线性关系。 结论 利用微悬臂梁传感技术对瘦肉精的检测是可行的。

    Abstract:

    Objective A novel technology of microcantilever sensor platform for label-free detection of clenbuterol antigen-antibody specificity binding is reported. Methods Thiolated clenbuterol antibody was immobilized on the gold-coated side of the microcantilever by self-assembled monolayer technique. Consequently the deflections of the microcantilever corresponding to the process of injecting different concentration of clenbuterol antigen were real-time monitored by optical lever technique. The activity of thiolated clenbuterol antibody and the clenbuterol antigen-antibody binding on the gold-coated side of the microcantilever were confirmed by an Enzyme-Linked Immunosorbent Assay (ELISA). Results The sensitivity of detecting clenbuterol is better than 1ng/ml. Microcantilevers functionalized with thiolated clenbuterol antibodies were exposed to 1 μg /ml of Chloramphenicol (CAP), and no significant response was detected, which confirmed the specificity of the immobilization method. In addition, clenbuterol antigen-antibody binding on the microcantilever generates a compressive surface stress and the surface stress is linear to logarithm of clenbuterol concentration over a range of concentration from 1ng/ml to 1μg/ml. Conclusions It is possible for detection of clenbuterol by microcantilever sensor platform.

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黄渊,薛长国,张青川,谭伟明,王保民,伍小平.利用微悬臂梁传感对瘦肉精进行非标记检测[J].医用生物力学,2009,24(2):89-93

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  • 收稿日期:2009-02-10
  • 最后修改日期:2009-02-20
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